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Learn about the efficacy and safety of Somavert, its tumour impact and its effect on co-morbidity management through clinical and real world data
Learn about funding and reimbursement for England, Scotland, Wales and Northern Ireland
Scroll through our resources about acromegaly management, patient resources, and experience with acromegaly
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Advice and support services to help you and your patients optimise your experience with Somavert about the efficacy and safety of Somavert through clinical and real world data
Click here for Somavert® (pegvisomant) Prescribing Information. Adverse event reporting information can be found at the bottom of the page.
Somavert is reimbursed by AWMSG, SMC and NI Formulary
In November 2017, the All Wales Medicines Strategy Group recommended Somavert as a third-line treatment of acromegaly in adults.
Somavert is recommended as an option for use within NHS Wales for the treatment of adult patients with acromegaly who have had an inadequate response to surgery and/or radiation therapy and in whom an appropriate medical treatment with SSAs didn’t normalise IGF-I concentrations or was not tolerated.
This recommendation applies only in circumstances where the approved Wales Patient Access Scheme (WPAS) is utilised or where the list/contract price is equivalent or lower than the WPAS price.
Following a second resubmission considered under the ultra-orphan process, pegvisomant (Somavert) is accepted for use within NHS Scotland.
For the treatment of adult patients with acromegaly who have had an inadequate response to surgery and/or radiation therapy and in whom an appropriate medical treatment with SSAs did not normalise IGF-I concentrations or was not tolerated.
SMC advice takes account of the benefits of a Patient Access Scheme (PAS) that improves the cost effectiveness of pegvisomant and is contingent upon the continuing availability of the PAS in NHS Scotland or a list price that is equivalent or lower. This advice takes account of the views from a Patient and Clinician Engagement (PACE) meeting.
In Northern Ireland, pegvisomant (Somavert) is accepted for use
For the treatment of adult patients with acromegaly who have had an inadequate response to surgery and/or radiation therapy and in whom an appropriate medical treatment with SSAs did not normalise IGF-I concentrations or was not tolerated
This advice takes account of the benefits of a Patient Access Scheme (PAS) that improves the cost effectiveness of pegvisomant and is contingent upon the continuing availability of the PAS in Northern Ireland or a list price that is equivalent or lower
We offer a range of services that help your patients at home with medication delivery and face-to-face support
To find out more about supporting your patients or to order starter kits
Abbrevations:
IGF-1=Insulin-like growth factor
NI formulation=Northern Ireland formulation
AWMSG=All Wales Medicine Stratergy Group
SMC=Scottish Medicines consortium
References
Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search
for MHRA Yellow Card in Google Play or Apple App Store
Adverse events should also be reported to Pfizer Medical Information on 01304 616161
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